157399-18-3

Upstream product

• 19249-03-7 triethylene glycol di-(p-toluenesulfonate) 
• 157399-21-8 2-hydroxyethyl 2,3,6-tri-O-benzyl-4-O-(2-hydroxyethyl)-α-D-glucopyranoside 
• 7464-56-4 1-O-allyl-α-D-glucopyranoside 
• 153097-69-9 allyl 2,3,6 tri-O-benzyl-α-D-glucopyranoside 
• 157399-20-7 allyl 4-O-allyl-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 87326-31-6 1-O-allyl-2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 100-44-7 benzyl chloride 
• 65987-12-4 1-O-allyl-4,6-O-benzylidene-α-D-glucopyranoside 

Relevant academic research and scientific papers

Chiral crown ethers incorporating D-glucose

A novel class of crown ether derivatives incorporating D-glucose and poly(ethylene glycol) units has been synthesized from allyl α-D-glucopyranoside by a simple and efficient strategy.The complexing properties of these compounds with alkali metal cations and ammonium ion have been evaluated by Cram's picrate method.Catalytic activity of macrocycle 2 in asymmetric Michael addition reaction was also studied.The average cavity size of these macrocycles was determined by the application of the MMX programme.